Pure Global AI
ANVISA registration 80105220328Active

Instrumento para preparo e processamento de amostras – fase pré-analítica

ANVISA Registration Number: 80105220328KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDADIYALAB ZJG BIOTECH CO., LTDRisk Class I
Verified
Device names
Technical name
Instrumento para preparo e processamento de amostras – fase pré-analítica
View exact technical-name matches →
Commercial name
Incubator DL061
View exact commercial-name matches →
Risk class
Class I
Registration details
Registration Number
80105220328
Process Number
25351148433202633
CNPJ
04299232000143
Company information
Registration Holder
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA
Manufacturer
DIYALAB ZJG BIOTECH CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Sep 28, 2026
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for Instrumento para preparo e processamento de amostras – fase pré-analítica in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80105220328 and manufactured by DIYALAB ZJG BIOTECH CO., LTD. The registration is held by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.